Key result
DNFCR-PF model improves heart failure mortality prediction over traditional Cox models, achieving a 0.66 C-index.
Why the study?
Existing models separately addressed frailty or competing risks in heart failure mortality prediction, but no deep learning approach had combined both to handle censored data and unobserved heterogeneity.
Does the DNFCR deep learning model improve cause-specific mortality prediction accuracy compared to traditional models in patients with HFrEF?
Cohort (n=435)
No
Does the DNFCR deep learning model improve cause-specific mortality prediction accuracy compared to traditional models in patients with HFrEF?
Effect estimate: ΔC-index 0.05 (95% CI 0.01-0.09)
Absolute Event Rate: 0.66% vs 0.61%
p-value: p=0.032
The DNFCR deep learning model, which integrates frailty and competing risks, demonstrated marginal but consistent improvements in predicting heart failure mortality compared to traditional survival models.
Hypothesis-generating for HFrEF mortality prediction; should not yet change practice without prospective validation.
This study presents a novel deep learning (DL) framework, the Deep Neural Frailty Competing Risks (DNFCR) model, which simultaneously integrates frailty and competing risks (CR) for mortality prediction in heart failure (HF). While existing models like Neural Frailty Models (NFM) address frailty and DeepHit handles CR, DNFCR is the first DL approach to combine both components, offering improved handling of censored data in healthcare applications. We evaluated DNFCR against established models (DeepSurv, CoxPH) using real-world HF data, assessing its ability to capture unobserved heterogeneity through proportional (DNFCR_PF) and non-proportional (DNFCR_NF) frailty structures. In this retrospective cohort study, we analyzed 435 HF patients (enrolled March-September 2018; 5-year follow-up until July 2023) with 57 demographic/clinical features, categorized by cause-specific mortality. The models' performance was evaluated using the C-index, IBS, and INBLL. Our results in mortality from heart failure demonstrated marginal but consistent improvements in predictive accuracy when incorporating frailty (C-index: ~0.66). Differences in predicting other-cause mortality were minimal across the models. DNFCR-PF also performed better regarding the IBS (0.17 ± 0.01) and INBLL (0.02 ± 0.53). However, the clinical relevance of the cause-specific mortality requires further validation in both outcome categories. Comparative analysis revealed that DNFCR and traditional models achieved comparable accuracy in survival prediction, highlighting that DL's superiority is context-dependent and influenced by data and unmeasured confounders. Strengths include DNFCR's potential for personalized risk stratification and adaptability to other diseases with CR. The DNFCR model showed DL potential in HF survival prediction but requires clinical validation compared to traditional approaches.
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Norouzi et al. (2025) conducted a cohort in Acute heart failure with reduced ejection fraction (HFrEF) (n=435). Deep Neural Frailty Competing Risks (DNFCR-PF) model vs. Cox proportional hazards (CoxPH) model was evaluated on C-index for mortality from heart failure (ΔC-index 0.05, 95% CI 0.01-0.09, p=0.032). The Deep Neural Frailty Competing Risks (DNFCR-PF) model improved the prediction of heart failure mortality compared to the traditional Cox proportional hazards model, achieving a C-index of 0.66.
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